Rapid2 Magnetic Stimulators (Magstim Rapid2, Magstim Super Rapid2, Magstim Super Rapid2 Plus1) (K250286)
Description
Rapid2 Magnetic Stimulators (Magstim Rapid2, Magstim Super Rapid2, Magstim Super Rapid2 Plus1) by The Magstim Company Limited, an FDA 510(k) cleared neurology device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K250286
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Rapid2 Magnetic Stimulators (Magstim Rapid2, Magstim Super Rapid2, Magstim Super Rapid2 Plus1) (K250286) cites 6 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K230014 | MagVenture Pain Therapy: MagPro R30, MagPro R30 with MagOpt... | Tonica Elektronik A/S | 2023 |
| K130403 | MAGSTIM DOUBLE 70-2 COIL | The Magstim Company , Ltd. | 2013 |
| K080499 | MAGSTIM DOUBLE 70MM AIR FILM COIL, MODEL 3910-00 | The Magstim Company , Ltd. | 2008 |
| K071821 | COILS, MODELS MCF-B65, MCF-75, MCF-125 AND COOL-B65 | Tonica Elektronik A/S | 2007 |
| K061645 | MAGPRO, MODEL R30 | Tonica Elektronik A/S | 2006 |
| K051864 | MAGSTIM RAPID2, MAGSTIM SUPER RAPID2, MODELS 3004-000, 3005-00 | The Magstim Company , Ltd. | 2005 |
Trace the full predicate network for K250286
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.